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Growth rate-dependent flexural rigidity of microtubules influences pattern formation in collective motion
BACKGROUND: Microtubules (MTs) are highly dynamic tubular cytoskeleton filaments that are essential for cellular morphology and intracellular transport. In vivo, the flexural rigidity of MTs can be dynamically regulated depending on their intracellular function. In the in vitro reconstructed MT-moto...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8287809/ https://www.ncbi.nlm.nih.gov/pubmed/34281555 http://dx.doi.org/10.1186/s12951-021-00960-y |
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author | Zhou, Hang Isozaki, Naoto Fujimoto, Kazuya Yokokawa, Ryuji |
author_facet | Zhou, Hang Isozaki, Naoto Fujimoto, Kazuya Yokokawa, Ryuji |
author_sort | Zhou, Hang |
collection | PubMed |
description | BACKGROUND: Microtubules (MTs) are highly dynamic tubular cytoskeleton filaments that are essential for cellular morphology and intracellular transport. In vivo, the flexural rigidity of MTs can be dynamically regulated depending on their intracellular function. In the in vitro reconstructed MT-motor system, flexural rigidity affects MT gliding behaviors and trajectories. Despite the importance of flexural rigidity for both biological functions and in vitro applications, there is no clear interpretation of the regulation of MT flexural rigidity, and the results of many studies are contradictory. These discrepancies impede our understanding of the regulation of MT flexural rigidity, thereby challenging its precise manipulation. RESULTS: Here, plausible explanations for these discrepancies are provided and a new method to evaluate the MT rigidity is developed. Moreover, a new relationship of the dynamic and mechanic of MTs is revealed that MT flexural rigidity decreases through three phases with the growth rate increases, which offers a method of designing MT flexural rigidity by regulating its growth rate. To test the validity of this method, the gliding performances of MTs with different flexural rigidities polymerized at different growth rates are examined. The growth rate-dependent flexural rigidity of MTs is experimentally found to influence the pattern formation in collective motion using gliding motility assay, which is further validated using machine learning. CONCLUSION: Our study establishes a robust quantitative method for measurement and design of MT flexural rigidity to study its influences on MT gliding assays, collective motion, and other biological activities in vitro. The new relationship about the growth rate and rigidity of MTs updates current concepts on the dynamics and mechanics of MTs and provides comparable data for investigating the regulation mechanism of MT rigidity in vivo in the future. GRAPHIC ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-021-00960-y. |
format | Online Article Text |
id | pubmed-8287809 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-82878092021-07-20 Growth rate-dependent flexural rigidity of microtubules influences pattern formation in collective motion Zhou, Hang Isozaki, Naoto Fujimoto, Kazuya Yokokawa, Ryuji J Nanobiotechnology Research BACKGROUND: Microtubules (MTs) are highly dynamic tubular cytoskeleton filaments that are essential for cellular morphology and intracellular transport. In vivo, the flexural rigidity of MTs can be dynamically regulated depending on their intracellular function. In the in vitro reconstructed MT-motor system, flexural rigidity affects MT gliding behaviors and trajectories. Despite the importance of flexural rigidity for both biological functions and in vitro applications, there is no clear interpretation of the regulation of MT flexural rigidity, and the results of many studies are contradictory. These discrepancies impede our understanding of the regulation of MT flexural rigidity, thereby challenging its precise manipulation. RESULTS: Here, plausible explanations for these discrepancies are provided and a new method to evaluate the MT rigidity is developed. Moreover, a new relationship of the dynamic and mechanic of MTs is revealed that MT flexural rigidity decreases through three phases with the growth rate increases, which offers a method of designing MT flexural rigidity by regulating its growth rate. To test the validity of this method, the gliding performances of MTs with different flexural rigidities polymerized at different growth rates are examined. The growth rate-dependent flexural rigidity of MTs is experimentally found to influence the pattern formation in collective motion using gliding motility assay, which is further validated using machine learning. CONCLUSION: Our study establishes a robust quantitative method for measurement and design of MT flexural rigidity to study its influences on MT gliding assays, collective motion, and other biological activities in vitro. The new relationship about the growth rate and rigidity of MTs updates current concepts on the dynamics and mechanics of MTs and provides comparable data for investigating the regulation mechanism of MT rigidity in vivo in the future. GRAPHIC ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12951-021-00960-y. BioMed Central 2021-07-19 /pmc/articles/PMC8287809/ /pubmed/34281555 http://dx.doi.org/10.1186/s12951-021-00960-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Zhou, Hang Isozaki, Naoto Fujimoto, Kazuya Yokokawa, Ryuji Growth rate-dependent flexural rigidity of microtubules influences pattern formation in collective motion |
title | Growth rate-dependent flexural rigidity of microtubules influences pattern formation in collective motion |
title_full | Growth rate-dependent flexural rigidity of microtubules influences pattern formation in collective motion |
title_fullStr | Growth rate-dependent flexural rigidity of microtubules influences pattern formation in collective motion |
title_full_unstemmed | Growth rate-dependent flexural rigidity of microtubules influences pattern formation in collective motion |
title_short | Growth rate-dependent flexural rigidity of microtubules influences pattern formation in collective motion |
title_sort | growth rate-dependent flexural rigidity of microtubules influences pattern formation in collective motion |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8287809/ https://www.ncbi.nlm.nih.gov/pubmed/34281555 http://dx.doi.org/10.1186/s12951-021-00960-y |
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